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Bioinformatics Institute of India
Contact No : Phone No. 0120-4320801 / 802 Mobile No. 9810535368, 9818473366
Email : info@bii.in, global@bii.in,
Website : www.bii.in
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Overview
About Us
 
Bioinformatics Institute of India has been setup as a premier institute, for the promotion, growth and prosperity of emerging life sciences domain. The institute has been promoted as an educational centre to conduct knowledge enhancement programs. The aim and vision of the institute is to provide a platform for individuals, professionals, R&D Organizations, Pharmaceutical & Software companies to utilize and harness the expertise professionals for new emerging business innovations.
 
The institute aims not only educational and research initiative but also vouch for creating a talent pool of professionals from various fields who can contribute for the growth and prosperity of Pharma / Clinical / Bioinformatics / Healthcare etc. as a career.
 
BII is the pioneer in the field of Bioinformatics and is today recognized across the globe as a premier institution offering programs in the area of Bioinformatics, Clinical Trials, Pharma Regulatory affairs, Pharma Quality Assurance and Control, Drug Design and Patenting, IPR and Biotechnology etc. BII offers its industry programs in different modes of education as mentioned below:
 
  • Regular Mode
  • Distance Mode
  • E-Learning
  • Propagate and promote among the members' strict adherence to IIMM code of Conduct and Ethics.
 
BII also conduct Workshops, Corporate trainings as per the industry demand to fill the gap between academia and industry. BII's another important initiative is its publication, India's first Bioinformatics Journal- "Bioinformatics Trends".

About Us

Bioinformatics Institute of India has been setup as a premier institute, for the promotion, growth and prosperity of emerging life sciences domain. The institute has been promoted as an educational centre to conduct knowledge enhancement programs. The aim and vision of the institute is to provide a platform for individuals, professionals, R&D Organizations, Pharmaceutical & Software companies to utilize and harness the expertise professionals for new emerging business innovations.

The institute aims not only educational and research initiative but also vouch for creating a talent pool of professionals from various fields who can contribute for the growth and prosperity of Pharma / Clinical / Bioinformatics / Healthcare etc. as a career .

BII is the pioneer in the field of Bioinformatics and is today recognized across the globe as a premier institution offering programs in the area of Bioinformatics, Clinical Trials, Pharma Regulatory affairs, Pharma Quality Assurance and Control, Drug Design and Patenting, IPR and Biotechnology etc. BII offers its industry programs in different modes of education as mentioned below:

  • Regular Mode
  • Distance Mode
  • E-Learning
  • Propagate and promote among the members' strict adherence to IIMM code of Conduct and Ethics.

BII also conduct Workshops, Corporate trainings as per the industry demand to fill the gap between academia and industry. BII's another important initiative is its publication, India's first Bioinformatics Journal- "Bioinformatics Trends".

 

 

 

Courses offered by Bioinformatics Institute of India All Courses 

Advance Program in Clinical Trial, Research & Data Management

Other Science

Category: Other Science Subjects

Degree: M.Sc.

Mode: Full Time

Medium: Campus

Duration: 6 Months

 

Traditional medical practice entails a doctor prescribing for a patient that treatment which in his judgment, based on past experience of himself and others, offers the best prognosis. Since there are.. Read more..


Industry Program in Clinical Trials Data Management & Pharmacovigilance

Other Science

Category: Other Science Subjects

Degree: M.Sc.

Mode: Correspondence

Medium: Distance Learning

Duration: 1 Year

 

With the globalization of the pharmaceutical industry, increased use of medicines and public awareness of safety issues have come forth with the challenges in four areas of operations—organizationa.. Read more..


Industry Program in Clinical Trial, Research & Administration

Category: Clinical Research

Degree: M.Sc.

Mode: Correspondence

Medium: Distance Learning

Duration: 1 Year

 

To be the biggest knowledge enhancement movement in the world in the area of Clinical Trial,Research & Administration. To spread, enhance and share knowledge in the emerging areas of.. Read more..


Industry Program in Pharma Quality Assurance and Quality Control

Other Science

Category: Other Science Subjects

Degree: M.Sc.

Mode: Correspondence

Medium: Distance Learning

Duration: 1 Year

 

Industry Program Pharma Quality Assurance and Quality Control- Distance Participation has been designed to enhance knowledge of professionals about the Quality Assurance in and Quality Control for.. Read more..


Industry Program in Pharmaceutical Marketing

Other Science

Category: Other Science Subjects

Degree: M.Sc.

Mode: Correspondence

Medium: Distance Learning

Duration: 1 Year

 

The biotechnology and pharmaceuticals industries have experienced rapid advances in science leading to the increasingly complex alliances between research and development, intense global competition,.. Read more..


Name : Bioinformatics Institute of India
Location : H-109 Sector 63
City : Noida
State : Uttar Pradesh
Country : India
Contact No : Phone No. 0120-4320801 / 802 Mobile No. 9810535368, 9818473366
Contact Email : info@bii.in, global@bii.in,
Website : www.bii.in 

Courses
Advance Program in Clinical Trial, Research & Data Management
View Program Details
Category : Other Science Subjects
Degree : M.Sc.
Mode : Full Time
Medium : Campus
Level : PG

Traditional medical practice entails a doctor prescribing for a patient that treatment which in his judgment, based on past experience of himself and others, offers the best prognosis. Since there are few conditions for which treatment is 100% effective, there is much scope for potential improvements in therapy and such improvements are derived via a clinical trial. Clinical Trial is a new emerging field in the area of pharmaceutical sciences or medical sciences. Clinical trials are research studies that test the effects of "health interventions" on people. Such health interventions are most commonly new drugs or treatments, though clinical trials may also examine the effects of other health interventions such as diagnostic methods, surgeries or procedures, technological devices, and educational methods. The main objective of the course is to provide students with a theoretical and practical understanding of the issues involved in the design, conduct, analysis and interpretation of clinical trials. Program Objectives The program would endow an introduction to the area of clinical trials, with more detailed coverage of some of the key issues to be considered in their design, analysis, documentation and interpretation. Further the course aims to develop: A theoretical and practical understanding of the issues involved in the design, conduct, analysis and interpretation of randomized controlled trials of health interventions. Skills to scrutinize information, to critically analyze and carry out research, and to communicate effectively. Describe the uses and applications of the main types of intervention studies: clinical trials and community trials. Describe the essential features and stages in the conduct of a clinical trial, and the role of randomization, use of placebo, blinding / masking and intention-to-treat analysis. Discuss the ethical issues involved in the conduct of a clinical trial. Program Methodology The prospective participants may join the program by submitting Application form with the necessary fees and attachments. The methodology for the program delivery would be: Delivery of the lectures by the technically expertise Faculty. Guest Faculty from industry and academia would deliver the lectures. Along with the theoretical knowledge student would also get a chance to have a practical oriented understanding of the subject e.g. role of computers in Clinical Trials E-learning platform via Moodle would also be employed for the classes. Students would also be taken for Industrial and Hospitals visits to have an overview of the entire Clinical trial process. Learning Outcome After completion of the course the participant would be able to: Have better understanding of Good Clinical Practice (GCP) and Standard Operating Procedures for Clinical Research. Participate in design, conduct and management of Global Clinical Trials, conducted at multicentric sites in India and Overseas. Contribute more effectively in their profession - pharmaceutical/Bio pharmaceutical companies in drug development. CRO's offering clinical research and clinical data management services, in BIO-IT Life science, Industry or Academic Research institutions. As a clinical investigator at hospitals, medical sites conducting trials on subjects. Handle regulatory affairs as per the changes in the statutory laws. Career Prospects Career prospects include a professional career in Clinical Research industry either as a clinical investigator, site coordinator in at a hospital conducting clinical investigations or CRO (Clinical Research Organization).Jobs are also available in pharmaceutical industry, drug development, medical writing, biostatistics or as a Manager of Clinical Project, Clinical Research Business Development, Clinical Operations, Data Management, Regulatory Affairs and Auditing of Clinical Trials. Careers in Clinical Research Clinical Research Associate Clinical Research Investigator Study Coordinator Data Manager / Biostatistician Regulatory Affairs Manager Clinical Trials Auditor Clinical Project Manager Clinical Research Manager Business Development Manager Drug Safety Associate Medical Writer

Industry Program in Clinical Trials Data Management & Pharmacovigilance
View Program Details
Category : Other Science Subjects
Degree : M.Sc.
Mode : Correspondence
Medium : Distance Learning
Level : PG

With the globalization of the pharmaceutical industry, increased use of medicines and public awareness of safety issues have come forth with the challenges in four areas of operations—organizational alignment, research & development , clinical trials data management, and risk & safety management. Thus in today’s biopharmaceutical product landscape, companies must be aware of crucial safety information about their products for which industry requires expertise and trained professionals in the domain related to clinical data management and safety monitoring department i.e. job profile like clinical data manager or Pharmaco-vigilance officer. BII to endow the knowledge in the area of clinical trials and Pharmaco-vigilance has introduced the “Industry Program in Clinical Trials Data Management and Pharmaco-vigilance”. Course Aims and Objectives :- The main objective of this course is to develop experts/skilled professionals to perform clinical data management tasks by having a correct spatial orientation of clinical research data management. The course will help participants to acquire a basic understanding of the concepts and practice of pharmaco-vigilance. The objectives of the course is to enable participants to understand issues surrounding the risks and benefits of drug used in humans including the cause, manifestations and consequences of adverse drug effects (ADEs).The aim of the course is to have thorough insight on project management related to pharmaco-vigilance /clinical data management domain .The regulatory perspectives of clinical trials & Pharmaco-vigilance are the important part of the course. Course-Curriculum :- Module I : Clinical Trials, Biostatistics and reporting analysis Module II : Clinical Trials Data Management Module III : Pharmaco-vigilance, Risk Management, Regulations and Compliance to Clinical Safety Module IV : Adverse Drug Reactions Reporting and Signal Detection Systems Module V : ICH-GCP Guidelines for Clinical Trials Module VI : Contract Research Module VII : Assurance and Control of Pharmaceutics Module VIII : Documentation and Medical Writing Module IX : Research Study Benefits of the course : - After the successful completion of this program, Students would be able to: Understand the regulatory perspectives on clinical research activities. Understand the protocol/study design and the database set-up. Perform database/procedure testing, data validation, SAE reconciliation and medical coding. Have a thorough insight on project management in data management domain. Understand how a pharmaco-vigilance and medical affairs team function and their dependency on data management. Career Opportunities : - The course caters to industry demands and moulds both fresher as well as experienced candidates to become exceptional professionals in the arena of clinical research and pharmaco-vigilance. The course also dwells on modulating invisible resources (communication-oral and written, decision-making, leadership qualities and time management skills) that would enable the participants to stand in a better stead than other candidates in the fiercely competitive job market. "Clinical data management" is a profession with increasing importance in product research and development process and is considered as an integral part of clinical trials. A career in both Pharmaco-vigilance and Data Management is bright for the sincere and diligent student and the working professional. Career opportunities in Pharmaco-vigilance includes as a Clinical Pharmaco-vigilance Officer. Clinical Pharmaco-vigilance Associate. Regulatory Affairs Associate. Clinical Drug Safety Associate and Clinical CRF Designer among others. For Data Management students, careers will be as Data Entry Operator, Research associates. Data coordinators and statisticians. Database Programmer. Database designer. Clinical data monitor. QA/QC executive. Project Manager.

Industry Program in Clinical Trial, Research & Administration
View Program Details
Category : Clinical Research
Degree : M.Sc.
Mode : Correspondence
Medium : Distance Learning
Level : PG

To be the biggest knowledge enhancement movement in the world in the area of Clinical Trial,Research & Administration. To spread, enhance and share knowledge in the emerging areas of Clinical Trial,Research & Administration. To provide quality inputs in the area of Clinical Trial,Research & Administration, to working professionals and individuals who have completed their education and willing to contribute in this area. To develop documentation / research writing expertise in the Clinical Trial,Research & Administration area. To equip participants of the BII Industry Program in Clinical Trial,Research & Administration to be able to spread awareness in this area by sharing their knowledge with others. To be a platform for interchange and exchange of knowledge in this area by organizing interaction Clinical Trial,Research & Administration Companies and program members. To make our country a hub for conduct of ethical Clinical Trial,Research & Administration leading to better opportunities and higher quality of life. Program Methodology :- Prospective Participants join the program by submitting participation form with necessary participation fee. Delivery of Program Kits and Participation material to the participant. The participant will go through the program kit and participation material by himself and through BII's centralized support. The participant with support of BII and his own initiative will participate in the program by: Self Study of Program Kit and other issued material Time Bound Preparation of a Research Report on the allocated topic through BII and his own resources (e.g employer, academic institution, library, internet etc). Submission of Research Report to BII . Time Bound Completion and Submission self analysis work books to BII . Interacting with other participating members and organizations through BII Blog at http://www.biinoida.blogspot.com Spreading awareness about Clinical Trial,Research & Administration area with others through knowledge sharing. Time Bound Completion of the Program Receiving Citation & Experience Certificate from BII about objectives achieved during the program. Program Areas :- Module I- Clinical Trials Module II- Contract Research Module III- Contract Research and Clinical Trial Environment Module IV- ICH -GCP Guidelines - International Conference of Harmonisation Module V- ICMR -Guidelines on Biomedical Research on Human Subjects Module VI- SCHEDULE Y Module VII- Biostatistics Module VIII- Research Study

Industry Program in Pharma Quality Assurance and Quality Control
View Program Details
Category : Other Science Subjects
Degree : M.Sc.
Mode : Correspondence
Medium : Distance Learning
Level : PG

Industry Program Pharma Quality Assurance and Quality Control- Distance Participation has been designed to enhance knowledge of professionals about the Quality Assurance in and Quality Control for Pharmaceutical Industry and Laboratories. The objective is to impart indepth and latest knowledge required for a Pharma Quality professional. The program covers topics like Quality Assurance and Control in Pharma Industry, WHO Good Manufacturing Practices, Inspection, Hazard and Risk Analysis, International Trade in Pharmaceuticals , Quality Standards, Quality Management, Auditing, Statistical Quality Control and Biostatistics, the ICH Guidelines, Indian Guidelines on GMP, Product Assessment and Registration, WHO Certification, Pharma Regulation Practices and Procedures etc. There is a good demand of Quality Control Officers all over the world. The program is conducted through Distance Participation. Program Objectives :- To be the biggest knowledge enhancement movement in the world in the area of Pharma QA & QC. To spread, enhance and share the knowledge in the emerging areas of Pharma QA & QC. To provide quality inputs in the area of Pharma QA&QC to working professionals and individuals who have completed their education and willing to contribute in this area. To develop documentation / research writing expertise in the Pharma QA & QC Domain. To equip participants of the BII Industry Program in Pharma QA &QC to be able to spread awareness in this area by sharing their knowledge with others. To be a platform for interchange and exchange of knowledge in this area by organizing interaction between the members of the program through BII Blog. Program Methodology :- Prospective Participants join the program by submitting participation form with necessary participation fee. Delivery of Program Kits and Participation material to the participant. The participant will go through the program kit and participation material by himself and through BII's centralized support. The participant with support of BII and his own initiative will participate in the program by: Self Study of Program Kit and other issued material Time Bound Preparation of a Research Report on the allocated topic through BII and his own resources (e.g employer, academic institution, library, internet etc). Submission of Research Report to BII . Time Bound Completion and Submission self analysis work books to BII . Interacting with other participating members and organizations through BII Blog at http://www.biinoida.blogspot.com Spreading awareness about Pharma QA & QC area with others through knowledge sharing. Time Bound Completion of the Program Receiving Citation & Experience Certificate from BII about objectives achieved during the program. Program Areas :- Module I : Quality Assurance in Pharma Industry-I Module II : Quality Assurance in Pharma Industry-II (WHO Perspective) Module III : Good Manufacturing Practices, Quality Assurance and Regulation Module IV : Quality Assurance and Control Module V : Pharma Regulation Practices & Procedures Module VI : Statistical Quality Control and Biostatistics Module VII : Research Study

Industry Program in Pharmaceutical Marketing
View Program Details
Category : Other Science Subjects
Degree : M.Sc.
Mode : Correspondence
Medium : Distance Learning
Level : PG

The biotechnology and pharmaceuticals industries have experienced rapid advances in science leading to the increasingly complex alliances between research and development, intense global competition, mega-mergers, and new regulations and shifts in policies. Any pharmaceutical company to progress and run successfully has to lead the company through this complex environment and need to understand the profound strategic implications of these changes i.e. to visualize them across the key functions of the business: discovery, marketing, finance, and business development. To cope up with the changing scenario pharma industry requires the professionals trained in the particular field like pharma marketing. With the aim of training the pharma professionals BII has introduced a program entitled as Industry Program in Pharmaceutical Marketing.Pharmaceutical Marketing is a industry specific course designed for pharmaceutical professionals keeping in view the skill set of the target audience and aimed developing the required technical expertise to hatrness the enormous employment opportunities thrown open in this. Course Aims and Objectives :- The objectives of the Pharmaceutical Marketing course are as mentioned below: To provide a specialized, high quality education as preparation for professional positions in pharmaceutical business, marketing and industry. To develop entrepreneurship skills to run a unit of operation or production and to develop entrepreneurship abilities for small scale drug sales and marketing. To develop entrepreneurship skills to run a unit of operation or production and to develop entrepreneurship abilities for small scale drug sales and marketing.. To gain and apply knowledge of scientific aspects in drug sales and marketing.. To impart systematic knowledge of basic and applied of pharmaceuticals marketing... Course-Curriculum :- Module I :Introduction to Pharmaceutics Module II :Pharma Product Management Module III : Pharmaceutical Marketing, logistics and Management Module IV :Human Resource Management Module V : Drug Design and Discovery Module VI : Emerging Areas of Pharma Industry: Clinical Trials and Contract Research Module VII : Pharma Practices, IPR and Procedures Module VIII : Business Research Methodology and Project

Industry Program in Drug Design and Patenting
View Program Details
Category : Other Science Subjects
Degree : M.Sc.
Mode : Correspondence
Medium : Distance Learning
Level : PG

Pharmaceutical Industry is the biggest beneficiary of Bioinformatics revolution. It has been found that pharmaceutical companies can simultaneously save significant money and time by integrating data and information across disciplines, pharmaceutical departments, processes and drugs. We are now moving into an era where drugs may be designed as per individual genetic profiles. Bioinformatics is now providing to be a powerful tool in the battle against toxicity and last-stage drug failures. Along with Bioinformatics discovery, development, marketing & manufacture of drugs is being transformed because of another change which is introduction of new patent systems & future multiple patent expires. This program is aimed at equipping professional respond to the above changes. The program is suitable for professionals & pharma students alike. Program Objectives :- To be the biggest knowledge enhancement movement in the world in the area of Drug Design and Patenting. To spread, enhance and share knowledge in the emerging areas of Drug Design and Patenting. To provide quality inputs in the area of Drug Design and Patenting to working professionals and individuals who have completed their education and willing to contribute in this area. To develop documentation / research writing expertise in the Drug Design and Patenting Domain. To equip participants of the BII Industry Program in Drug Design and Patenting to be able to spread awareness in this area by sharing their knowledge with others. To be a platform for interchange and exchange of knowledge in this area by organizing interaction between program members through BII Blog. Program Methodology :- Prospective Participants join the program by submitting admission form with necessary participation fee. Delivery of Program Kits and Support material to the participant. The participant will go through the program kit and support material by himself and through BII's centralized support. The participant with the support of BII and his own initiative will participate in the program by: Self Study of Program Kit and other helping material Time Bound Preparation of a Research Report on the allocated topic through BII and his own resources (e.g employer, academic institution, library, internet etc). Submission of Research Report to BII . Time Bound Completion and Submission self analysis work books to BII . Interacting with other participating members and organizations through BII Blog at http://www.biinoida.blogspot.com Spreading awareness about Drug Design and Patenting area with others through knowledge sharing. Time Bound Completion of the Program Receiving Citation & Experience Certificate from BII about objectives achieved during the program. Program Areas :- Module I : Drug Discovery Basics Module II : Drug Design and Discovery Module III : Patenting Module IV : Indian Patent Laws and Pharmaceutical Industry Module V : Cheminformatics Module VI : Cheminformatics Database Design and Their Management Module VII : Research Study

Industry Program in Pharmaceutical Chemistry and Production
View Program Details
Category : Other Science Subjects
Degree : M.Sc.
Mode : Correspondence
Medium : Distance Learning
Level : PG

The objective of Industry Program in Pharmaceutical Chemistry and Production-Distance Learning program is to provide an intensive and up to date learning in the emerging area of Chemical sciences. The program provides a basic to advance level of expertise in Industry Program in Pharmaceutical Chemistry and Production and its usage in the industry. Program curriculum :- Paper 1 - Pharmaceutical Chemistry Paper 2 - Medicinal Chemistry Paper 3 -Modern Combinatorial Chemistry Paper 4 -Pharmaceutical Manufacturing Paper 5 -Pharmaceutical Analysis, Evaluation & Testing Paper 6 -Drug Design & discovery

Program in Pharma Good Manufacturing Practices
View Program Details
Category : Other Medicine Certificate Courses
Degree : Certificate
Mode : Correspondence
Medium : Distance Learning
Level : Certification

Program Objectives :- To provide a better understanding and an overview of appropriate standards and practices for product testing, manufacturing, storage, handling and distribution. To ensure an effective overall approach to product quality control and risk management. To understand the practices and requirements before going for a license. To understand the definitions of common terms used in this industry. To be aware of some of the Code of Federal Regulations. To expand the pharmaceutical business in any international capacity. To develop documentation / research writing expertise in the Pharma Good Manufacturing Practices area. To provide quality inputs in the area of Pharma Good Manufacturing Practices, to working professionals and individuals who have completed their education and willing to contribute in this area. To make available to Industry a pool of competent professionals in the area of Pharma Good Manufacturing Practices. Program Methodology :- Prospective Participants join the program by submitting participation form with necessary participation fee. Delivery of Program Kits and Participation material to the participant. The participant will go through the program kit and participation material by himself and through BII's centralized support. The participant, with support of BII and his own initiative, will participate in the program by: Self Study of Program Kit and other issued material. Time Bound Preparation of a Research Report on the allocated topic through BII and his own resources (e.g employer, academic institution, library, internet etc). Submission of Research Report to BII. Time Bound Completion and Submission of program assignments to BII. Interacting with other participating members and organizations through BII Portal Spreading awareness about Pharma Good Manufacturing Practices with others through knowledge sharing. Time Bound Completion of the Program. Receiving Citation & Experience Certificate from BII about objectives achieved during the program. Program Areas :- Module I- Good Manufacturing Practices, Quality Assurance And Regulation Module II- Quality Assurance And Control Module III- Quality Assurance of Pharmaceuticals Module IV- SCHEDULE M

Industry Program in Intellectual Property Rights
View Program Details
Category : Other Medicine Certificate Courses
Degree : Certificate
Mode : Correspondence
Medium : Distance Learning
Level : Certification

Program Objectives :- To spread, enhance and share the knowledge in the Intellectual Property Rights. To provide quality inputs in the area of Intellectual Property Rights, to working professionals and individuals who have completed their education and willing to contribute in this area. To develop documentation / specification / claim writing expertise in the area of Intellectual Property Rights. To equip participants of the BII Industry Program in Intellectual Property Rights to be able to spread awareness in this area by sharing the knowledge with others. To be a platform for interchange and exchange of knowledge in this area by organizing interaction with Companies and program members. To make available a pool of competent professionals in the area of Intellectual Property Rights. Program Methodology :- Prospective Participants join the program by submitting participation form with necessary participation fee. Delivery of Program Kits and Participation material to the participant. The participant will go through the program kit and participation material by himself and through BII's centralized support. The participant with support of BII and his own initiative will participate in the program by: Self Study of Program Kit and other issued material. Time Bound Preparation of a Research Report on the allocated topic through BII and his own resources (e.g employer, academic institution, library, internet etc). Submission of Research Report to BII . Time Bound Completion and Submission self analysis work books to BII . Interacting with other participating members and organizations through BII Blog at http://www.biinoida.blogspot.com Spreading awareness about Intellectual Property Rights Ares with others through knowledge sharing. Time Bound Completion of the Program Receiving Citation & Experience Certificate from BII about objectives achieved during the program. Program Areas :- Module I- Biomedical Intellectual Property Management Module II- Biotechnology Regulation Module III- Intellectual Property Law Module IV- Intellectual Property Rights

Related Question and Answer
Q & A
Contact
Name : Bioinformatics Institute of India
Location : H-109 Sector 63
City : Noida
State : Uttar Pradesh
Country : India
Contact No : Phone No. 0120-4320801 / 802 Mobile No. 9810535368, 9818473366
Contact Email : info@bii.in, global@bii.in,
Website : www.bii.in   
Courses
Advance Program in Clinical Trial, Research & Data Management
View Program Details
Category : Other Science Subjects
Degree : M.Sc.
Mode : Full Time
Medium : Campus
Level : PG

Traditional medical practice entails a doctor prescribing for a patient that treatment which in his judgment, based on past experience of himself and others, offers the best prognosis. Since there are few conditions for which treatment is 100% effective, there is much scope for potential improvements in therapy and such improvements are derived via a clinical trial. Clinical Trial is a new emerging field in the area of pharmaceutical sciences or medical sciences. Clinical trials are research studies that test the effects of "health interventions" on people. Such health interventions are most commonly new drugs or treatments, though clinical trials may also examine the effects of other health interventions such as diagnostic methods, surgeries or procedures, technological devices, and educational methods. The main objective of the course is to provide students with a theoretical and practical understanding of the issues involved in the design, conduct, analysis and interpretation of clinical trials. Program Objectives The program would endow an introduction to the area of clinical trials, with more detailed coverage of some of the key issues to be considered in their design, analysis, documentation and interpretation. Further the course aims to develop: A theoretical and practical understanding of the issues involved in the design, conduct, analysis and interpretation of randomized controlled trials of health interventions. Skills to scrutinize information, to critically analyze and carry out research, and to communicate effectively. Describe the uses and applications of the main types of intervention studies: clinical trials and community trials. Describe the essential features and stages in the conduct of a clinical trial, and the role of randomization, use of placebo, blinding / masking and intention-to-treat analysis. Discuss the ethical issues involved in the conduct of a clinical trial. Program Methodology The prospective participants may join the program by submitting Application form with the necessary fees and attachments. The methodology for the program delivery would be: Delivery of the lectures by the technically expertise Faculty. Guest Faculty from industry and academia would deliver the lectures. Along with the theoretical knowledge student would also get a chance to have a practical oriented understanding of the subject e.g. role of computers in Clinical Trials E-learning platform via Moodle would also be employed for the classes. Students would also be taken for Industrial and Hospitals visits to have an overview of the entire Clinical trial process. Learning Outcome After completion of the course the participant would be able to: Have better understanding of Good Clinical Practice (GCP) and Standard Operating Procedures for Clinical Research. Participate in design, conduct and management of Global Clinical Trials, conducted at multicentric sites in India and Overseas. Contribute more effectively in their profession - pharmaceutical/Bio pharmaceutical companies in drug development. CRO's offering clinical research and clinical data management services, in BIO-IT Life science, Industry or Academic Research institutions. As a clinical investigator at hospitals, medical sites conducting trials on subjects. Handle regulatory affairs as per the changes in the statutory laws. Career Prospects Career prospects include a professional career in Clinical Research industry either as a clinical investigator, site coordinator in at a hospital conducting clinical investigations or CRO (Clinical Research Organization).Jobs are also available in pharmaceutical industry, drug development, medical writing, biostatistics or as a Manager of Clinical Project, Clinical Research Business Development, Clinical Operations, Data Management, Regulatory Affairs and Auditing of Clinical Trials. Careers in Clinical Research Clinical Research Associate Clinical Research Investigator Study Coordinator Data Manager / Biostatistician Regulatory Affairs Manager Clinical Trials Auditor Clinical Project Manager Clinical Research Manager Business Development Manager Drug Safety Associate Medical Writer

Industry Program in Clinical Trials Data Management & Pharmacovigilance
View Program Details
Category : Other Science Subjects
Degree : M.Sc.
Mode : Correspondence
Medium : Distance Learning
Level : PG

With the globalization of the pharmaceutical industry, increased use of medicines and public awareness of safety issues have come forth with the challenges in four areas of operations—organizational alignment, research & development , clinical trials data management, and risk & safety management. Thus in today’s biopharmaceutical product landscape, companies must be aware of crucial safety information about their products for which industry requires expertise and trained professionals in the domain related to clinical data management and safety monitoring department i.e. job profile like clinical data manager or Pharmaco-vigilance officer. BII to endow the knowledge in the area of clinical trials and Pharmaco-vigilance has introduced the “Industry Program in Clinical Trials Data Management and Pharmaco-vigilance”. Course Aims and Objectives :- The main objective of this course is to develop experts/skilled professionals to perform clinical data management tasks by having a correct spatial orientation of clinical research data management. The course will help participants to acquire a basic understanding of the concepts and practice of pharmaco-vigilance. The objectives of the course is to enable participants to understand issues surrounding the risks and benefits of drug used in humans including the cause, manifestations and consequences of adverse drug effects (ADEs).The aim of the course is to have thorough insight on project management related to pharmaco-vigilance /clinical data management domain .The regulatory perspectives of clinical trials & Pharmaco-vigilance are the important part of the course. Course-Curriculum :- Module I : Clinical Trials, Biostatistics and reporting analysis Module II : Clinical Trials Data Management Module III : Pharmaco-vigilance, Risk Management, Regulations and Compliance to Clinical Safety Module IV : Adverse Drug Reactions Reporting and Signal Detection Systems Module V : ICH-GCP Guidelines for Clinical Trials Module VI : Contract Research Module VII : Assurance and Control of Pharmaceutics Module VIII : Documentation and Medical Writing Module IX : Research Study Benefits of the course : - After the successful completion of this program, Students would be able to: Understand the regulatory perspectives on clinical research activities. Understand the protocol/study design and the database set-up. Perform database/procedure testing, data validation, SAE reconciliation and medical coding. Have a thorough insight on project management in data management domain. Understand how a pharmaco-vigilance and medical affairs team function and their dependency on data management. Career Opportunities : - The course caters to industry demands and moulds both fresher as well as experienced candidates to become exceptional professionals in the arena of clinical research and pharmaco-vigilance. The course also dwells on modulating invisible resources (communication-oral and written, decision-making, leadership qualities and time management skills) that would enable the participants to stand in a better stead than other candidates in the fiercely competitive job market. "Clinical data management" is a profession with increasing importance in product research and development process and is considered as an integral part of clinical trials. A career in both Pharmaco-vigilance and Data Management is bright for the sincere and diligent student and the working professional. Career opportunities in Pharmaco-vigilance includes as a Clinical Pharmaco-vigilance Officer. Clinical Pharmaco-vigilance Associate. Regulatory Affairs Associate. Clinical Drug Safety Associate and Clinical CRF Designer among others. For Data Management students, careers will be as Data Entry Operator, Research associates. Data coordinators and statisticians. Database Programmer. Database designer. Clinical data monitor. QA/QC executive. Project Manager.

Industry Program in Clinical Trial, Research & Administration
View Program Details
Category : Clinical Research
Degree : M.Sc.
Mode : Correspondence
Medium : Distance Learning
Level : PG

To be the biggest knowledge enhancement movement in the world in the area of Clinical Trial,Research & Administration. To spread, enhance and share knowledge in the emerging areas of Clinical Trial,Research & Administration. To provide quality inputs in the area of Clinical Trial,Research & Administration, to working professionals and individuals who have completed their education and willing to contribute in this area. To develop documentation / research writing expertise in the Clinical Trial,Research & Administration area. To equip participants of the BII Industry Program in Clinical Trial,Research & Administration to be able to spread awareness in this area by sharing their knowledge with others. To be a platform for interchange and exchange of knowledge in this area by organizing interaction Clinical Trial,Research & Administration Companies and program members. To make our country a hub for conduct of ethical Clinical Trial,Research & Administration leading to better opportunities and higher quality of life. Program Methodology :- Prospective Participants join the program by submitting participation form with necessary participation fee. Delivery of Program Kits and Participation material to the participant. The participant will go through the program kit and participation material by himself and through BII's centralized support. The participant with support of BII and his own initiative will participate in the program by: Self Study of Program Kit and other issued material Time Bound Preparation of a Research Report on the allocated topic through BII and his own resources (e.g employer, academic institution, library, internet etc). Submission of Research Report to BII . Time Bound Completion and Submission self analysis work books to BII . Interacting with other participating members and organizations through BII Blog at http://www.biinoida.blogspot.com Spreading awareness about Clinical Trial,Research & Administration area with others through knowledge sharing. Time Bound Completion of the Program Receiving Citation & Experience Certificate from BII about objectives achieved during the program. Program Areas :- Module I- Clinical Trials Module II- Contract Research Module III- Contract Research and Clinical Trial Environment Module IV- ICH -GCP Guidelines - International Conference of Harmonisation Module V- ICMR -Guidelines on Biomedical Research on Human Subjects Module VI- SCHEDULE Y Module VII- Biostatistics Module VIII- Research Study

Industry Program in Pharma Quality Assurance and Quality Control
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Category : Other Science Subjects
Degree : M.Sc.
Mode : Correspondence
Medium : Distance Learning
Level : PG

Industry Program Pharma Quality Assurance and Quality Control- Distance Participation has been designed to enhance knowledge of professionals about the Quality Assurance in and Quality Control for Pharmaceutical Industry and Laboratories. The objective is to impart indepth and latest knowledge required for a Pharma Quality professional. The program covers topics like Quality Assurance and Control in Pharma Industry, WHO Good Manufacturing Practices, Inspection, Hazard and Risk Analysis, International Trade in Pharmaceuticals , Quality Standards, Quality Management, Auditing, Statistical Quality Control and Biostatistics, the ICH Guidelines, Indian Guidelines on GMP, Product Assessment and Registration, WHO Certification, Pharma Regulation Practices and Procedures etc. There is a good demand of Quality Control Officers all over the world. The program is conducted through Distance Participation. Program Objectives :- To be the biggest knowledge enhancement movement in the world in the area of Pharma QA & QC. To spread, enhance and share the knowledge in the emerging areas of Pharma QA & QC. To provide quality inputs in the area of Pharma QA&QC to working professionals and individuals who have completed their education and willing to contribute in this area. To develop documentation / research writing expertise in the Pharma QA & QC Domain. To equip participants of the BII Industry Program in Pharma QA &QC to be able to spread awareness in this area by sharing their knowledge with others. To be a platform for interchange and exchange of knowledge in this area by organizing interaction between the members of the program through BII Blog. Program Methodology :- Prospective Participants join the program by submitting participation form with necessary participation fee. Delivery of Program Kits and Participation material to the participant. The participant will go through the program kit and participation material by himself and through BII's centralized support. The participant with support of BII and his own initiative will participate in the program by: Self Study of Program Kit and other issued material Time Bound Preparation of a Research Report on the allocated topic through BII and his own resources (e.g employer, academic institution, library, internet etc). Submission of Research Report to BII . Time Bound Completion and Submission self analysis work books to BII . Interacting with other participating members and organizations through BII Blog at http://www.biinoida.blogspot.com Spreading awareness about Pharma QA & QC area with others through knowledge sharing. Time Bound Completion of the Program Receiving Citation & Experience Certificate from BII about objectives achieved during the program. Program Areas :- Module I : Quality Assurance in Pharma Industry-I Module II : Quality Assurance in Pharma Industry-II (WHO Perspective) Module III : Good Manufacturing Practices, Quality Assurance and Regulation Module IV : Quality Assurance and Control Module V : Pharma Regulation Practices & Procedures Module VI : Statistical Quality Control and Biostatistics Module VII : Research Study

Industry Program in Pharmaceutical Marketing
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Category : Other Science Subjects
Degree : M.Sc.
Mode : Correspondence
Medium : Distance Learning
Level : PG

The biotechnology and pharmaceuticals industries have experienced rapid advances in science leading to the increasingly complex alliances between research and development, intense global competition, mega-mergers, and new regulations and shifts in policies. Any pharmaceutical company to progress and run successfully has to lead the company through this complex environment and need to understand the profound strategic implications of these changes i.e. to visualize them across the key functions of the business: discovery, marketing, finance, and business development. To cope up with the changing scenario pharma industry requires the professionals trained in the particular field like pharma marketing. With the aim of training the pharma professionals BII has introduced a program entitled as Industry Program in Pharmaceutical Marketing.Pharmaceutical Marketing is a industry specific course designed for pharmaceutical professionals keeping in view the skill set of the target audience and aimed developing the required technical expertise to hatrness the enormous employment opportunities thrown open in this. Course Aims and Objectives :- The objectives of the Pharmaceutical Marketing course are as mentioned below: To provide a specialized, high quality education as preparation for professional positions in pharmaceutical business, marketing and industry. To develop entrepreneurship skills to run a unit of operation or production and to develop entrepreneurship abilities for small scale drug sales and marketing. To develop entrepreneurship skills to run a unit of operation or production and to develop entrepreneurship abilities for small scale drug sales and marketing.. To gain and apply knowledge of scientific aspects in drug sales and marketing.. To impart systematic knowledge of basic and applied of pharmaceuticals marketing... Course-Curriculum :- Module I :Introduction to Pharmaceutics Module II :Pharma Product Management Module III : Pharmaceutical Marketing, logistics and Management Module IV :Human Resource Management Module V : Drug Design and Discovery Module VI : Emerging Areas of Pharma Industry: Clinical Trials and Contract Research Module VII : Pharma Practices, IPR and Procedures Module VIII : Business Research Methodology and Project

Industry Program in Drug Design and Patenting
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Category : Other Science Subjects
Degree : M.Sc.
Mode : Correspondence
Medium : Distance Learning
Level : PG

Pharmaceutical Industry is the biggest beneficiary of Bioinformatics revolution. It has been found that pharmaceutical companies can simultaneously save significant money and time by integrating data and information across disciplines, pharmaceutical departments, processes and drugs. We are now moving into an era where drugs may be designed as per individual genetic profiles. Bioinformatics is now providing to be a powerful tool in the battle against toxicity and last-stage drug failures. Along with Bioinformatics discovery, development, marketing & manufacture of drugs is being transformed because of another change which is introduction of new patent systems & future multiple patent expires. This program is aimed at equipping professional respond to the above changes. The program is suitable for professionals & pharma students alike. Program Objectives :- To be the biggest knowledge enhancement movement in the world in the area of Drug Design and Patenting. To spread, enhance and share knowledge in the emerging areas of Drug Design and Patenting. To provide quality inputs in the area of Drug Design and Patenting to working professionals and individuals who have completed their education and willing to contribute in this area. To develop documentation / research writing expertise in the Drug Design and Patenting Domain. To equip participants of the BII Industry Program in Drug Design and Patenting to be able to spread awareness in this area by sharing their knowledge with others. To be a platform for interchange and exchange of knowledge in this area by organizing interaction between program members through BII Blog. Program Methodology :- Prospective Participants join the program by submitting admission form with necessary participation fee. Delivery of Program Kits and Support material to the participant. The participant will go through the program kit and support material by himself and through BII's centralized support. The participant with the support of BII and his own initiative will participate in the program by: Self Study of Program Kit and other helping material Time Bound Preparation of a Research Report on the allocated topic through BII and his own resources (e.g employer, academic institution, library, internet etc). Submission of Research Report to BII . Time Bound Completion and Submission self analysis work books to BII . Interacting with other participating members and organizations through BII Blog at http://www.biinoida.blogspot.com Spreading awareness about Drug Design and Patenting area with others through knowledge sharing. Time Bound Completion of the Program Receiving Citation & Experience Certificate from BII about objectives achieved during the program. Program Areas :- Module I : Drug Discovery Basics Module II : Drug Design and Discovery Module III : Patenting Module IV : Indian Patent Laws and Pharmaceutical Industry Module V : Cheminformatics Module VI : Cheminformatics Database Design and Their Management Module VII : Research Study

Industry Program in Pharmaceutical Chemistry and Production
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Category : Other Science Subjects
Degree : M.Sc.
Mode : Correspondence
Medium : Distance Learning
Level : PG

The objective of Industry Program in Pharmaceutical Chemistry and Production-Distance Learning program is to provide an intensive and up to date learning in the emerging area of Chemical sciences. The program provides a basic to advance level of expertise in Industry Program in Pharmaceutical Chemistry and Production and its usage in the industry. Program curriculum :- Paper 1 - Pharmaceutical Chemistry Paper 2 - Medicinal Chemistry Paper 3 -Modern Combinatorial Chemistry Paper 4 -Pharmaceutical Manufacturing Paper 5 -Pharmaceutical Analysis, Evaluation & Testing Paper 6 -Drug Design & discovery

Program in Pharma Good Manufacturing Practices
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Category : Other Medicine Certificate Courses
Degree : Certificate
Mode : Correspondence
Medium : Distance Learning
Level : Certification

Program Objectives :- To provide a better understanding and an overview of appropriate standards and practices for product testing, manufacturing, storage, handling and distribution. To ensure an effective overall approach to product quality control and risk management. To understand the practices and requirements before going for a license. To understand the definitions of common terms used in this industry. To be aware of some of the Code of Federal Regulations. To expand the pharmaceutical business in any international capacity. To develop documentation / research writing expertise in the Pharma Good Manufacturing Practices area. To provide quality inputs in the area of Pharma Good Manufacturing Practices, to working professionals and individuals who have completed their education and willing to contribute in this area. To make available to Industry a pool of competent professionals in the area of Pharma Good Manufacturing Practices. Program Methodology :- Prospective Participants join the program by submitting participation form with necessary participation fee. Delivery of Program Kits and Participation material to the participant. The participant will go through the program kit and participation material by himself and through BII's centralized support. The participant, with support of BII and his own initiative, will participate in the program by: Self Study of Program Kit and other issued material. Time Bound Preparation of a Research Report on the allocated topic through BII and his own resources (e.g employer, academic institution, library, internet etc). Submission of Research Report to BII. Time Bound Completion and Submission of program assignments to BII. Interacting with other participating members and organizations through BII Portal Spreading awareness about Pharma Good Manufacturing Practices with others through knowledge sharing. Time Bound Completion of the Program. Receiving Citation & Experience Certificate from BII about objectives achieved during the program. Program Areas :- Module I- Good Manufacturing Practices, Quality Assurance And Regulation Module II- Quality Assurance And Control Module III- Quality Assurance of Pharmaceuticals Module IV- SCHEDULE M

Industry Program in Intellectual Property Rights
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Category : Other Medicine Certificate Courses
Degree : Certificate
Mode : Correspondence
Medium : Distance Learning
Level : Certification

Program Objectives :- To spread, enhance and share the knowledge in the Intellectual Property Rights. To provide quality inputs in the area of Intellectual Property Rights, to working professionals and individuals who have completed their education and willing to contribute in this area. To develop documentation / specification / claim writing expertise in the area of Intellectual Property Rights. To equip participants of the BII Industry Program in Intellectual Property Rights to be able to spread awareness in this area by sharing the knowledge with others. To be a platform for interchange and exchange of knowledge in this area by organizing interaction with Companies and program members. To make available a pool of competent professionals in the area of Intellectual Property Rights. Program Methodology :- Prospective Participants join the program by submitting participation form with necessary participation fee. Delivery of Program Kits and Participation material to the participant. The participant will go through the program kit and participation material by himself and through BII's centralized support. The participant with support of BII and his own initiative will participate in the program by: Self Study of Program Kit and other issued material. Time Bound Preparation of a Research Report on the allocated topic through BII and his own resources (e.g employer, academic institution, library, internet etc). Submission of Research Report to BII . Time Bound Completion and Submission self analysis work books to BII . Interacting with other participating members and organizations through BII Blog at http://www.biinoida.blogspot.com Spreading awareness about Intellectual Property Rights Ares with others through knowledge sharing. Time Bound Completion of the Program Receiving Citation & Experience Certificate from BII about objectives achieved during the program. Program Areas :- Module I- Biomedical Intellectual Property Management Module II- Biotechnology Regulation Module III- Intellectual Property Law Module IV- Intellectual Property Rights

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Name : Bioinformatics Institute of India
Location : H-109 Sector 63
City : Noida
State : Uttar Pradesh
Country : India
Contact No : Phone No. 0120-4320801 / 802 Mobile No. 9810535368, 9818473366
Contact Email : info@bii.in, global@bii.in,
Website : www.bii.in   
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